iUUCD 2.0 - integrated annotations for ubiquitin and ubiquitin-like conjugation database

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs27139	snp	G/T	0.487871	0.076925	intron-variant	PPWD1	GRCh38.p7	5:65585354	AGATAATGAATAAAG[G/T]GTCATGCTGAGATTA	23398
rs27140	snp	A/G	0.487809	0.0771174	intron-variant	PPWD1	GRCh38.p7	5:65585751	TAACTGGCTTTATTT[A/G]GGTTATTGAGAAAGA	23398
rs27141	snp	A/G	0.470103	0.118552	synonymous-codon	PPWD1	GRCh38.p7	5:65586109	ACGACATGACAGGCC[A/G]TACACACTCAGCATG	23398
rs27142	snp	A/C	0.487746	0.0773096	downstream-variant-500B	PPWD1	GRCh38.p7	5:65588028	TTTAATTTTGAATAC[A/C]TGCCAGATATTCCGC	23398
rs36223	snp	C/T	0	0	intron-variant	PPWD1	GRCh38.p7	5:65570148	GAAAATTAGATACAG[C/T]GAAGCCTTATAATGT	23398
rs36224	snp	A/G	0.487809	0.0771174	intron-variant	PPWD1	GRCh38.p7	5:65570767	AGGGAAGAAGGAAAG[A/G]GAGATCTTTTTTTCT	23398
rs36225	snp	C/T	0.47934	0.0995154	intron-variant	PPWD1	GRCh38.p7	5:65571099	TTCACAGATATTGAA[C/T]GTTTGCCCTTTGAGA	23398
rs37333	snp	G/T	0.377582	0.214995	intron-variant	PPWD1	GRCh38.p7	5:65578561	gtatcttgttttagt[G/T]tggatttccctggca	23398
rs37334	snp	G/T	0.374	0.217081	intron-variant	PPWD1	GRCh38.p7	5:65579278	AATTGATACCTTTTG[G/T]GGGGTAGAGAAACAC	23398
rs37335	snp	A/G	0.377385	0.215112	intron-variant	PPWD1	GRCh38.p7	5:65580562	tctgttgcccaggct[A/G]gagtgcagtgacgtg	23398
rs37336	snp	A/G	0.377385	0.215112	intron-variant	PPWD1	GRCh38.p7	5:65580663	ggattataggtgcat[A/G]ccaccatacccagct	23398
rs37337	snp	C/T	0.487809	0.0771174	intron-variant	PPWD1	GRCh38.p7	5:65581028	GTTAGGAAATGACTA[C/T]AGCATTACAGTATAT	23398
rs37338	snp	A/T	0.487809	0.0771174	intron-variant	PPWD1	GRCh38.p7	5:65581164	TCTAAATGGGTAAAT[A/T]CTTTTAAGATGAGAA	23398
rs37339	snp	A/G	0.487809	0.0771174	intron-variant	PPWD1	GRCh38.p7	5:65582076	ACTGGAGAATAGGAT[A/G]TTAAGGTGATAGCAT	23398
rs37340	snp	C/T	0.487684	0.0775019	intron-variant	PPWD1	GRCh38.p7	5:65583775	GCAACACGGCAAGAC[C/T]CTATCTCTTAAAAAA	23398
rs41353	snp	C/T	0.487809	0.0771174	intron-variant	PPWD1	GRCh38.p7	5:65577317	TTGTTAAAAAAAACA[C/T]ACAACAACTTGAAAC	23398
rs41354	snp	G/T	0.487809	0.0771174	intron-variant	PPWD1	GRCh38.p7	5:65578229	ggatgtaccacagtt[G/T]atccattcacgtact	23398
rs149208	snp	A/G	0.473359	0.112298	intron-variant	PPWD1	GRCh38.p7	5:65569578	TGCTTTGGGAATACT[A/G]AGTGATTCATAGATC	23398
rs149512	snp	A/T	0.493201	0.0579089	intron-variant	PPWD1	GRCh38.p7	5:65569519	TAATAGGTTTTTTTT[A/T]AAAAAAAACCCTTCT	23398
rs149513	snp	G/T	0	0	intron-variant	PPWD1	GRCh38.p7	5:65582248	TAAAGAAACAGGCCT[G/T]GAGAAGTCCAGAGTT	23398
rs151717	snp	G/T	0	0	intron-variant	PPWD1	GRCh38.p7	5:65582209	ACATCAGATAGAGGT[G/T]GCTTAGGAGAGAGCA	23398
rs152063	snp	A/C	0.487809	0.0771174	intron-variant, utr-variant-5-prime	PPWD1	GRCh38.p7	5:65568830	TTCTAGTCTCAAGTT[A/C]TCAGTGTGGTAAAAC	23398
rs154946	snp	A/C/G	0.408521	0.219172	intron-variant	PPWD1	GRCh38.p7	5:65576468	AATCGCTTGAACCTA[A/C/G]GAGGCAGACGCTGCA	23398
rs154948	snp	A/G	0.377187	0.215229	intron-variant	PPWD1	GRCh38.p7	5:65575306	CCTGCAAAATGTGTA[A/G]TCCAGCATCCTAGGC	23398
rs154949	snp	A/G	0.487809	0.0771174	intron-variant	PPWD1	GRCh38.p7	5:65575267	CTGAGTCTTCTCTCC[A/G]GCAGAAATGATCATT	23398
rs154950	snp	A/G	0.487809	0.0771174	intron-variant, utr-variant-5-prime	PPWD1	GRCh38.p7	5:65568397	CATTTTAGAGATGAC[A/G]AAACTGAAGTTTAGA	23398
rs154951	snp	A/G	0.487809	0.0771174	intron-variant	PPWD1	GRCh38.p7	5:65569241	GTTGAATTTTGTTGC[A/G]TATGAAAGTAGTATG	23398
rs155064	snp	A/T	0.468349	0.121752	intron-variant	PPWD1	GRCh38.p7	5:65578301	acctgtacacagatg[A/T]ttatagcagctttta	23398
rs173487	snp	A/C	0.31357	0.241783	intron-variant	PPWD1	GRCh38.p7	5:65574760	AGAGATTTGTGCCGG[A/C]CGGGCGCGGTGGCTC	23398
rs183044	snp	G/T	0	0	intron-variant	PPWD1	GRCh38.p7	5:65565976	CTTTAACATGTTCTT[G/T]GGACATTGGACTGTT	23398
rs185013	snp	A/G	0.487809	0.0771174	intron-variant	PPWD1	GRCh38.p7	5:65574618	AAATTAGCCGGGCGC[A/G]GTGGCGGGCGCCTGT	23398
rs185477	snp	G/T	0	0	intron-variant	PPWD1	GRCh38.p7	5:65576032	cagcatatctcagtt[G/T]ggactagccatctat	23398
rs187409	snp	A/G	0.487809	0.0771174	intron-variant	PPWD1	GRCh38.p7	5:65574919	AATGAGAGTTTGCCA[A/G]AAAAGCCAACCATCA	23398
rs192189	snp	A/G	0.487746	0.0773096	intron-variant	PPWD1	GRCh38.p7	5:65574518	CGCGATTGAGCCACT[A/G]CAGTCCGCAGTCCGG	23398
rs193274	snp	G/T	0	0	intron-variant	PPWD1	GRCh38.p7	5:65565991	TGGACATTGGACTGT[G/T]GTATATATTTTCAGA	23398
rs261247	snp	A/G	0.487809	0.0771174	intron-variant, upstream-variant-2KB	PPWD1	GRCh38.p7	5:65566375	TTGGAACTGGGATAT[A/G]ACTGCTGTAATCTTA	23398
rs261248	snp	C/T	0.487809	0.0771174	intron-variant	PPWD1	GRCh38.p7	5:65566101	GTGGACAAATACTTA[C/T]TAAGAACACAATACG	23398
rs261249	snp	A/C	0.492693	0.0882035	intron-variant	PPWD1	GRCh38.p7	5:65566092	TACTTACTAAGAACA[A/C]AATACGTTCTAGGTC	23398
rs261250	snp	A/G	0.313814	0.241719	upstream-variant-2KB, intron-variant	CENPK, PPWD1	GRCh38.p7	5:65564720	AGTAAGGGGTTGGGA[A/G]AGGAAGGTAATGGAA	23398
rs261251	snp	A/G	0.485118	0.0849685	upstream-variant-2KB, intron-variant	CENPK, PPWD1	GRCh38.p7	5:65564275	AGTTTTTTAAGGGAA[A/G]GTGCTAAAGTACGAT	23398
rs261252	snp	A/T	0.358034	0.225452	upstream-variant-2KB, intron-variant	CENPK, PPWD1	GRCh38.p7	5:65563765	ACTAACATTTTCCTA[A/T]TCTTATGTGTTTGGC	23398
rs261253	snp	C/T	0.498632	0.0261223	intron-variant, upstream-variant-2KB	CENPK, PPWD1	GRCh38.p7	5:65561236	ATTCATGATGACTGA[C/T]TTTGGCTTTGTGAAC	23398
rs353312	snp	G/T	0.0201999	0.0984476	intron-variant	PPWD1	GRCh38.p7	5:65565983	ATGTTCTTTGGACAT[G/T]GGACTGTTGTATATA	23398
rs402645	snp	C/G	0.499846	0.00878459	upstream-variant-2KB	CENPK, PPWD1	GRCh38.p7	5:65563200	TTGGATGTGCTCATT[C/G]CCACCCCAGCCAATC	23398
rs432206	snp	C/G	0.499928	0.00598999	intron-variant, upstream-variant-2KB, utr-variant-5-prime	CENPK, PPWD1	GRCh38.p7	5:65562860	GAAAACATGTTTAGT[C/G]CATCTGAAAGGAAAC	23398
rs433041	snp	G/T			downstream-variant-500B	PPWD1	GRCh38.p7	5:65587883	ACTTTATCATAGATA[G/T]ATATATATGAAAACA	23398
rs436185	snp	A/C	0	0	intron-variant	PPWD1	GRCh38.p7	5:65573864	AGTGATGGCTAGAGT[A/C]ACTCTTTCAAAATAT	23398
rs456564	snp	A/T	0.37778	0.214877	intron-variant, upstream-variant-2KB	PPWD1	GRCh38.p7	5:65567169	TTTCATGGAACTTTT[A/T]AATTTTTTTTCCTTT	23398
rs460262	snp	G/T	0.487746	0.0773096	intron-variant, upstream-variant-2KB	PPWD1	GRCh38.p7	5:65568005	ATGAGTAGGTTCGTG[G/T]AGAAGGATAATAATA	23398
rs461534	snp	G/T	0.484841	0.0857308	upstream-variant-2KB, intron-variant	CENPK, PPWD1	GRCh38.p7	5:65564097	ATACGATGGGCTGAG[G/T]CTTTTTGTCACTAAC	23398
rs461780	snp	A/G	0.487809	0.0771174	intron-variant	PPWD1	GRCh38.p7	5:65574490	CGGCCTGGGCAACAG[A/G]GCGAGACTCCGTCTC	23398
rs467362	snp	C/T	0.487746	0.0773096	intron-variant, upstream-variant-2KB	PPWD1	GRCh38.p7	5:65567861	GAGTGAACCAGGTAG[C/T]GTCTGAGCTTCCCTG	23398
rs467436	snp	A/T	0.484841	0.0857308	upstream-variant-2KB, intron-variant	CENPK, PPWD1	GRCh38.p7	5:65564099	ACGATGGGCTGAGTC[A/T]TTTTGTCACTAACGA	23398
rs468821	snp	A/G	0.487809	0.0771174	intron-variant	PPWD1	GRCh38.p7	5:65573797	TGGAGATAGAATCAT[A/G]AGTTAAAACAGATCA	23398
rs582627	snp	C/T			intron-variant	PPWD1	GRCh38.p7	5:65579204	TGAggccaggcacgg[C/T]ggctcacacctgtaa	23398
rs626485	snp	C/T	0	0	intron-variant	PPWD1	GRCh38.p7	5:65579196	tgctgggattacagg[C/T]gtgagccaccgtgcc	23398
rs626503	snp	C/T			intron-variant	PPWD1	GRCh38.p7	5:65579212	gtgagccgccgtgcc[C/T]ggccTCATTTCTGTT	23398
rs669571	snp	A/G	0.487933	0.0767327	intron-variant, upstream-variant-2KB	PPWD1	GRCh38.p7	5:65566985	AGGATGTTCTCAGGC[A/G]TAAAAATCTAAGAAT	23398
rs1309794	snp	A/T			intron-variant	PPWD1	GRCh38.p7	5:65573554	ttttttttttttttt[A/T]agtacagacgggttt	23398
rs1611096	in-del	-/CAAA	0.487809	0.0771174	intron-variant	PPWD1	GRCh38.p7	5:65576192	TCTAGTAACATTAAA[-/CAAA]GTATAAAGAAAACAG	23398
rs2546061	snp	C/T					GRCh38.p7	5:65578766	atatatatgtatata[C/T]atatacacatatatg	23398
rs3752673	snp	C/T	0.367058	0.220901	intron-variant	PPWD1	GRCh38.p7	5:65569831	AATCATGCACACTTA[C/T]TTTACTGTTATTTAC	23398
rs3752674	snp	A/G	0.0886198	0.190936	intron-variant	PPWD1	GRCh38.p7	5:65570021	TTTTTAAAAGTATAT[A/G]TATTTTAACTTATTG	23398
rs3756301	snp	G/T	0.293037	0.246268	intron-variant, upstream-variant-2KB	PPWD1	GRCh38.p7	5:65567458	AAATAAACCAAATAC[G/T]ATTTTGTATTTTCTT	23398
rs6862211	snp	C/G	0.145305	0.227022	intron-variant	PPWD1	GRCh38.p7	5:65574751	TACAGGCGTGAGCCA[C/G]CGCGCCCGGCCGGCA	23398
rs6867890	snp	A/G	0.0174175	0.0916809	intron-variant	PPWD1	GRCh38.p7	5:65575573	TGGGACAGAAGTCTG[A/G]CTTATTTTCATCTGC	23398
rs6879928	snp	C/G	0.0410537	0.137264	intron-variant	PPWD1	GRCh38.p7	5:65570681	gttccatcagggttt[C/G]atttctgatgagggc	23398
rs7379716	snp	A/T			intron-variant	PPWD1	GRCh38.p7	5:65573477	tatatatatatatat[A/T]ttttttttattagag	23398
rs9686195	snp	G/T	0	0	intron-variant	PPWD1	GRCh38.p7	5:65583991	CGTAAGGGCTTCAAT[G/T]GAAAAAAAGGTGAAC	23398
rs9686777	snp	C/T			intron-variant, upstream-variant-2KB	PPWD1	GRCh38.p7	5:65566820	TCCATCCCTTTCTTT[C/T]TTTTTTTTTTTTTGC	23398
rs9687917	snp	A/G	0	0	intron-variant	PPWD1	GRCh38.p7	5:65583992	GTAAGGGCTTCAATT[A/G]AAAAAAAGGTGAACA	23398
rs9790869	snp	G/T	0.371987	0.218218	intron-variant, upstream-variant-2KB	CENPK, PPWD1	GRCh38.p7	5:65562753	GTCTTTTGGTTATTT[G/T]AAGTAGCTGCTTCTC	23398
rs9791024	snp	A/C	0.370974	0.218781	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	CENPK, PPWD1	GRCh38.p7	5:65563128	AACTCCAGGTCGCCT[A/C]GGCGCTGCGCAGGAA	23398
rs9885586	snp	A/G	0.00755907	0.0610114	intron-variant, utr-variant-5-prime	PPWD1	GRCh38.p7	5:65568694	ggtggattACTTTAC[A/G]CTTTTTTAGATCAGT	23398
rs10053248	snp	A/T	0	0	intron-variant	PPWD1	GRCh38.p7	5:65579231	CTCATTTCTGTTTTT[A/T]AACCTGAAAATTATA	23398
rs10514984	snp	A/G	0.124837	0.216412	intron-variant, upstream-variant-2KB	CENPK, PPWD1	GRCh38.p7	5:65562553	CAAATACAGCTTGTC[A/G]AAATGACCTCCGTAA	23398
rs10560318	in-del	-/ACAC			intron-variant, upstream-variant-2KB	CENPK, PPWD1	GRCh38.p7	5:65561616	CACACACACACACAC[-/ACAC]TTAAGAGTTGAACTT	23398
rs10592952	in-del	-/GG			upstream-variant-2KB, intron-variant	CENPK, PPWD1	GRCh38.p7	5:65564061	AAACCCGAAGTCTGT[-/GG]TTTTGAAATCACGCT	23398
rs10682457	in-del	-/A/AA	0.5	0	intron-variant	PPWD1	GRCh38.p7	5:65584889	TATGAAAAAAAAAAA[-/A/AA]CAACTGTCCTTCTGA	23398
rs10940044	snp	A/G	0.438105	0.164671	intron-variant	PPWD1	GRCh38.p7	5:65578808	tatacatatatatgt[A/G]tatatatatactttt	23398
rs11282501	in-del	-/TGTTAA	0.473543	0.111932	intron-variant	PPWD1	GRCh38.p7	5:65576119	CTCAATTTTTTATAT[-/TGTTAA]TGTTGAGATGATATT	23398
rs11740053	snp	A/G	0.369754	0.219451	intron-variant	PPWD1	GRCh38.p7	5:65581787	AGCTTTATACAGCTA[A/G]CATTGTTACGAATTT	23398
rs11743237	snp	C/T			intron-variant	PPWD1	GRCh38.p7	5:65573324	taattaatttatttt[C/T]tgagacagagttgca	23398
rs11952433	snp	C/T	0.145305	0.227022	intron-variant, upstream-variant-2KB	PPWD1	GRCh38.p7	5:65566692	TACATATAATTCTCC[C/T]CTCCCCTCGTTCCCT	23398
rs11957149	snp	A/G	0.145305	0.227022	upstream-variant-2KB, intron-variant	CENPK, PPWD1	GRCh38.p7	5:65564841	GAATAATTTCCCTCA[A/G]CTCTTCCACTGAACT	23398
rs11959161	snp	G/T	0.145305	0.227022	intron-variant	PPWD1	GRCh38.p7	5:65581215	ATTATTACTAAAAAT[G/T]TATTAGTATATGAAG	23398
rs12516229	snp	C/G	0.36955	0.219562	intron-variant	PPWD1	GRCh38.p7	5:65565444	TAAACTTAATATAAC[C/G]GAGACAGATATAAAT	23398
rs12520386	snp	C/T	0	0	intron-variant	PPWD1	GRCh38.p7	5:65576674	gccaccatgcccagc[C/T]TGAAATACTATTTTT	23398
rs12652387	snp	A/G	0	0	downstream-variant-500B	PPWD1	GRCh38.p7	5:65587614	AATGGACTAAACTCA[A/G]GCAAATAGCACTCAT	23398
rs13160139	snp	A/G	0.00472811	0.0483911	intron-variant	PPWD1	GRCh38.p7	5:65580999	TATGTCTTCTTCACT[A/G]TTAAATCCAGAAAGT	23398
rs13161135	snp	C/T	0.118933	0.212888	intron-variant	PPWD1	GRCh38.p7	5:65575822	ACCTAATGGTAATCT[C/T]ACTGCCCTGTGTCAG	23398
rs13167170	snp	A/C	0	0	missense, intron-variant, utr-variant-5-prime	PPWD1	GRCh38.p7	5:65569983	ACTTTGACATGATCA[A/C]CATGCTGAAACTTGG	23398
rs13167188	snp	A/C			intron-variant	PPWD1	GRCh38.p7	5:65570029	AGTATATATATTTTA[A/C]CTTATTGAAGTAATT	23398
rs13167303	snp	A/C	0	0	intron-variant	PPWD1	GRCh38.p7	5:65570060	TGTAAATCAGACTTT[A/C]CCATTTAATAGGTTA	23398
rs13167451	snp	A/C	0.118584	0.212673	intron-variant	PPWD1	GRCh38.p7	5:65570094	CTAAATAGTATATTA[A/C]CATATCTTTAAATAA	23398
rs13167480	snp	A/C	0	0	intron-variant	PPWD1	GRCh38.p7	5:65570210	CACAGAAATTTCTAA[A/C]CAGCATCATAACAAG	23398
rs13167526	snp	C/G	0	0	missense, intron-variant, utr-variant-5-prime	PPWD1	GRCh38.p7	5:65569943	GTGGGTGATGATAAA[C/G]CAATGAAGGTGTTTG	23398
rs13177756	snp	A/G	0.293037	0.246268	intron-variant	PPWD1	GRCh38.p7	5:65579177	CTGCCTCGGCCTCCC[A/G]AAGTGCTGGGATTAC	23398
rs13187337	snp	G/T			synonymous-codon, intron-variant, utr-variant-5-prime	PPWD1	GRCh38.p7	5:65569996	CAACATGCTGAAACT[G/T]GGGTGAGTCTTTTTA	23398
rs13187647	snp	G/T	0	0	intron-variant	PPWD1	GRCh38.p7	5:65570185	GCATCTGCTATGATT[G/T]GTTATCAATCACAGA	23398

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